JPH0462667B2 - - Google Patents
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- Publication number
- JPH0462667B2 JPH0462667B2 JP604086A JP604086A JPH0462667B2 JP H0462667 B2 JPH0462667 B2 JP H0462667B2 JP 604086 A JP604086 A JP 604086A JP 604086 A JP604086 A JP 604086A JP H0462667 B2 JPH0462667 B2 JP H0462667B2
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
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- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
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- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
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- 229910000838 Al alloy Inorganic materials 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 229940053200 antiepileptics fatty acid derivative Drugs 0.000 description 1
- 229910000963 austenitic stainless steel Inorganic materials 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003302 ferromagnetic material Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000010365 information processing Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 230000005415 magnetization Effects 0.000 description 1
- 229940002712 malachite green oxalate Drugs 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
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- 229920000573 polyethylene Polymers 0.000 description 1
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- 238000010298 pulverizing process Methods 0.000 description 1
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- AZJPTIGZZTZIDR-UHFFFAOYSA-L rose bengal Chemical compound [K+].[K+].[O-]C(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 AZJPTIGZZTZIDR-UHFFFAOYSA-L 0.000 description 1
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- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- XOSXWYQMOYSSKB-LDKJGXKFSA-L water blue Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC(C=C2)=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C(C=C2)=CC=C2S([O-])(=O)=O)=CC(S(O)(=O)=O)=C1N.[Na+].[Na+] XOSXWYQMOYSSKB-LDKJGXKFSA-L 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Magnetic Brush Developing In Electrophotography (AREA)
- Developing For Electrophotography (AREA)
Description
〔産業上の利用分野〕
本発明は画像担体表面に形成した静電潜像の非
帯電領域に一成分系の磁性トナーを付着させて反
転トナー像を得る反転現像方法に関するものであ
り、特に冷間圧力定着可能の磁性トナーを使用す
る反転現像方法に関する。
〔従来の技術〕
近年情報処理機器の高性能化および多様化に伴
つて、出力形態も多様化、高速化を要求され、ノ
ンインパクト型式の電子写真方式のプリンタが開
発されている。上記プリンタの記録原理は一般の
電子複写機と同様、画像担体表面に形成した静電
潜像を現像後、普通紙へ転写するものである。而
してプリンタにおいては、コンピユータからの情
報を一様帯電させた画像担体表面にレーザ光など
で書き込み、この書き込み部すなわち露光部にト
ナーを付着させるため、反転現像を行う必要があ
る。
上記の反転現像に使用する現像剤としては、磁
性キヤリアとトナーとからなる二成分系現像剤が
一般的である。この方法では普通紙へのトナー像
の静電転写が可能であり、高画質のプリンタ画像
が得られるが、キヤリアとトナーとの混合比率を
一定にするための手段が必要である。従つて現像
装置の大型化、複雑化を招来する他、キヤリアを
定期的に交換する必要があるという欠点がある。
このような欠点解消のために、磁性を有するト
ナー粒子のみからなる一成分系現像剤を使用して
静電潜像を現像する方式がある。上記磁性トナー
を使用する反転現像方法においては、静電潜像と
同極性の電荷を有する磁性トナーを保持する導電
性スリーブに、静電潜像と同極性の直流バイアス
電圧を印加することにより、トナーを非画像部に
付着させるのである。また現像によつて得られた
トナー像を転写シート上に静電転写する場合、電
気抵抗の高い絶縁性磁性トナーを使用するのが一
般的である。
〔発明が解決しようとする問題点〕
上記のような荷電型の絶縁性磁性トナーを、静
電潜像と同極性に帯電させて反転現像を行つた場
合、画質が二成分系現像剤を使用したものより劣
るのが実情である。すなわち静電潜像と同極性に
帯電する磁性トナーを使用する場合には、画像濃
度の点では前記二成分系現像剤を使用するものと
同等の結果が得られるのであるが、解像度の点で
充分でなく、また画像周辺にチリが発生し易いと
いう問題点がある。
本発明は上記のような問題点を解決し、磁性ト
ナーを使用した反転現像方法であり、解像度が高
く、かつ画像周辺にチリが発生することのない反
転現像方法を提供することを目的とするものであ
る。
〔問題点を解決するための手段〕
上記問題点を解決するために、本発明において
は下記のような技術的手段を採用した。すなわ
ち、
A. 画像担体表面に静電潜像を形成し、前記画
像担体表面に対向して配置しかつ内部に磁界発
生部材を備えた非磁性導電性スリーブ上に樹脂
と磁性粉を主体とする磁性トナーを供給し、前
記スリーブと前記磁界発生部材との相対的回転
により前記磁性トナーを前記画像担体表面に向
かつて搬送し、前記スリーブに直流電圧を印加
して前記静電潜像の非画像部に前記磁性トナー
を付着させる反転現像方法において。
B.前記画像担体の負の帯電特性とする。
C. 前記磁性トナーを冷間圧力定着可能でありか
つ正帯電特性とする。
D. 前記スリーブに負の直流電圧を印加する。
という技術的手段を講じたものである。
〔作用〕
第1図は本発明を実施するための現像装置の一
例を示す要部断面図である。同図において1は感
光体ドラムであり、静電潜像(図中−記号で示
す)を保持する光導電性層1aと、電気的に接地
された導電性基体1bとからなり、矢印W方向に
回転自在に設ける。次に2はトナー槽でありトナ
ー3を収容する。而してトナー槽2の下部には感
光体ドラム1と対向してスリーブ4を回転自在に
設けると共に、スリーブ4内には表面に複数個の
磁極を有する永久磁石部材5を同軸的かつ矢印X
方向に独立回転自在に設ける。6はドクターブレ
ードであり、前記スリーブ4の表面に臨ませて出
入自在に設け、スリーブ4上を移動するトナー3
の厚さを規制する。次にスリーブ4は例えばオー
ステナイト系ステンレス鋼またはアルミニウム合
金等の非磁性かつ導電性材料によつて形成し、負
の極性を有する直流電源7と電気的に接続する。
上記のような構成により反転現像方法について
記述する。まずスリーブ4と永久磁石部材5とを
相対的に回転させることにより、トナー槽2内に
収容したトナー3をスリーブ4上に引き出し、矢
印Y方向にドクターギヤツプdから現像ギヤツプ
Dに向かつて搬送する。トナー3は光導電性槽1
a上に形成した静電潜像と逆極性の正帯電する特
性を付与してあり、上記搬送過程においてスリー
ブ4、ドクターブレード6またはトナー3同志の
接触により正の電荷を持つようになる。而して正
電荷を有するトナー3が現像領域に到達すると、
光導電性層1aの非画像部に付着してトナー像を
形成する。次にこのトナー像は感光体ドラム1の
回転によつて転写位置に至り、転写シート(図示
せず)の裏面から静電潜像と逆極正の正の電界を
印加することにより、転写シート上に転写され、
次いで圧力定着手段によつて定着されるのであ
る。
本発明の反転現像方法においては、静電潜像と
逆極性に帯電する性質の磁性トナーを使用するも
のであるため、磁性トナーは静電潜像の画像部に
付着するように思考されるが、本発明者等の実験
によれば、前記のように静電潜像の非画像部に明
確に付着することが確認され、再現性もまた充分
に存在する。
本発明により高品質の画像が得られる理由は、
詳細は不明であるが、次のようなこであると推察
される。
磁性トナーはスリーブ上を搬送される過程で、
上述したように正極性に帯電し、殆どのトナー粒
子は正の電荷を持つようになる。この磁性トナー
が現像領域に至り、静電潜像の電界中に入ると、
電界の方向に従つてトナー中の電荷が移動し、静
電潜像電位の低い感光体との界面近接にあるトナ
ー粒子は負の電荷を持つようになる。これにより
負の電荷を持つたトナー粒子が静電潜像の非画像
部に付着して、反転画像が得られる。従つて、従
来は静電潜像と同極性に帯電する磁性トナーを使
用していたため過現像状態を惹起する。即ちトナ
ーが感光体表面に付着しすぎる結果、チリが発生
する。これに対し、本発明によれば、感光体との
界面近傍にあるトナーのみが現像に寄与する帯電
極性となるため、過現像が抑制され、チリの発生
を防止することができると思われる。
本発明において使用する磁性トナーは、ブロー
オフ法によつて測定した場合の摩擦帯電量が2〜
20μc/gであり、スリーブ上の帯電電圧が5〜
60Vであるのが望ましい。すなわち摩擦帯電量お
よび帯電電圧が過大になると、画像濃度が低下
し、一方これらが不足すると、カブリが多くな
り、何れも不都合である。
次に磁性トナーを構成する磁性粉としては、フ
エライト、マグネタイトを始めとする鉄、コバル
ト、ニツケル等の強磁性を示す元素を含む合金ま
たは化合物およびその他熱処理若しくは何等かの
処理によつて強磁性を示す種々の合金等を使用し
得る。これらの強磁性体は、数μmないし数十μm
の粒径を有するトナー中に含有させるため、平均
粒系が0.02〜3μmのものが望ましい。而してトナ
ー中に含有させる量は、トナー全量に対し30〜70
重量%とするのが望ましい。30重量%未満ではト
ナーの磁力が低下してスリーブから飛散し易くな
り、一方70重量%を越えると、樹脂含有量が極め
て少なくなつて定着性が低下してしまうので不都
合である。
次に本発明において使用する磁性トナーは、冷
間圧力定着可能のものであり、例えば下記のよう
な樹脂を使用する。すなわち、高級脂肪酸類、高
級脂肪酸金属塩類、高級脂肪酸誘導体、高級脂肪
酸アミド類、ワツクス類、ロジン誘導体、アルキ
ツド樹脂、エポキシ変性フエノール樹脂、天然樹
脂変性フエノール樹脂、アミノ樹脂、シリコン樹
脂、ポリウレタン、ユリア樹脂、ポリエステル樹
脂、アクリル酸またはメタクリル酸と長鎖アルキ
ルアクリレート共重合オリゴマー、スチレンと長
鎖アルキルアクリレート、長鎖アルキルメタクリ
レートとの共重合オリゴマー、ポリオレフイン、
エチレン〜酢酸ビニル共重合体、エチレン〜ビニ
ルアルキルエーテル共重合体、無水マレイン酸系
共重合体、石油系残渣、ゴム類等が挙げられる。
上記の樹脂は何れも任意に選定し、また任意に
混合して使用できるが、トナーとして形成した場
合の流動性を低下させないために、ガラス転移点
が40℃を越えるものが有効である。
而して上記以外にも、一般の乾式現像剤として
使用されている種々の顔料および/または添料を
添加含有させることができる。しかしトナー全量
に対する含有量は、トナーの電気特性等を考慮し
て10重量%未満が適当である。使用できる顔料と
しては、例えばカーボンブラツク、アニリンブル
ー、カルコオイルブルー、クロームイエロー、ウ
ルトラマリンブルー、デユポンオイルレツド、キ
ノリンイエロー、メチレンブルークロラド、フタ
ロシアニンブルー、マラカイトグリーンオクサレ
ート、ランプブラツク、ローズベンガルおよびそ
れ等の混合物等である。なおマグネタイトのよう
に磁性紛自体が着色している場合には敢て添加す
る必要はない。またカーボンフラツクを使用する
場合には、トナーの絶縁性を低下させないため
に、トナー中の樹脂成分100重量部当たり0.01〜
5重量部の範囲で含有させるのが望ましい。
次に本発明において使用する磁性トナーは、上
記の材料により粉砕法若しくはスプレードライ法
等の公知の方法によつて製造できる。而して生成
すべきトナーの平均粒径は、5〜30μm、好まし
くは10〜20μmの範囲がよい。なお分級後のトナ
ー粒子表面には、例えばカーボンブラツク若しく
は酸化錫等の導電性粒子またはシリカ粉末等の添
加剤の添加により、電気抵抗若しくは流動性を調
節することができる。
〔実施例〕
以下本発明を実施例によつて具体的に説明する
が、本発明はこれらの例によつて限定されるもの
ではない。
ポリエチレンワツクス(三井石油化学工業製
HIWA×200P)とエチレン酢酸ビニル共重合体
(アライドケミカル社製ACP400)とを重量比
7:3で混合した樹脂、マグネタイト(戸田工業
製EPT500)および正の荷電制御剤(オリエント
化学製ボントロンNo..1)とを表に示す配合によ
つて乾式混合し、ニーダで200℃の温度で加熱混
練した。生成した混練物を冷却・固化後ジエツト
ミルにより20μm以下の粒子に粉砕した。次にこ
の粉砕粉をスーパーミキサーに投入し、更に微粉
末シリカ(日本アエロジル製R972)を0.1〜0.5重
量部添加して混合した。混合粉を120℃の熱気流
中に導入して熱処理を行つた後、ジグザグ分級機
によつて分級を行い5〜20μmの粒度分布を有す
る磁性トナーNo..1〜4を得た。これらの磁性ト
ナーの摩擦帯電量(以下TECと記す)および表
面電位は表に示す通りである。
而して上記磁性トナーのTECは、市販のブロ
ーオフ粉体帯電量測定器(東芝ケミカル製TB−
200)により、次の条件で測定した値である。キ
ヤリア(日本鉄粉製Z−200)10gとトナー0.5g
を外径40mmφのプラスチツク容器に投入し、流動
表面角度測定器にて10分間回転させ、得られた混
合物の中から200mgの試料を採取し、325メツシユ
の篩を使用した容器に投入し、前記帯電量測定器
によりブロー圧1.0Kg/mm2、ブロー時間40秒の条
件で測定する。
またトナーの帯電電圧すなわち表面電位は第2
図に示す装置によつて測定する。同図において、
8は非磁性スリーブ(外径50mmφ)、9は永久磁
石部材(外径46mmφ、長さ150mm、12極対称着磁、
スリーブ上の磁束密度1000G)、10は表面電位
計(トレツク344)、11は測定子である。而
してスリーブ8と測定子11との間隙gを5mmに
調整した後、スリーブ8上にトナーを3g供給
し、永久磁石部材9を1000rpmで1分間回転させ
た時のトナーの表面電位を測定する。
次にTECおよび表面電位の異なる磁性トナー
No..5〜7を前記実施例と同様の条件で作製し
た。なお、No..5の磁性トナーは負の荷電制御剤
(オリエント化学製ボントロンE81)を使用して
いる点が他のトナーと異なる。
[Industrial Field of Application] The present invention relates to a reversal development method for obtaining a reversal toner image by depositing a one-component magnetic toner on the uncharged area of an electrostatic latent image formed on the surface of an image carrier. The present invention relates to a reversal development method using magnetic toner that can be fixed under pressure. [Prior Art] In recent years, as information processing equipment has become more sophisticated and diversified, there has been a demand for diversified output formats and faster speeds, and non-impact electrophotographic printers have been developed. The recording principle of the printer described above is similar to that of general electronic copying machines, in which an electrostatic latent image formed on the surface of an image carrier is developed and then transferred to plain paper. In printers, information from a computer is written on the uniformly charged surface of an image carrier using a laser beam or the like, and in order to attach toner to the written area, that is, the exposed area, it is necessary to perform reversal development. The developer used in the above reversal development is generally a two-component developer consisting of a magnetic carrier and a toner. Although this method enables electrostatic transfer of toner images onto plain paper and provides high-quality printer images, it requires a means to maintain a constant mixing ratio of carrier and toner. Therefore, there is a drawback that the developing device becomes larger and more complicated, and the carrier needs to be replaced periodically. In order to overcome these drawbacks, there is a method of developing an electrostatic latent image using a one-component developer consisting only of magnetic toner particles. In the above reversal development method using magnetic toner, a DC bias voltage of the same polarity as the electrostatic latent image is applied to a conductive sleeve holding magnetic toner having a charge of the same polarity as the electrostatic latent image. This causes the toner to adhere to the non-image area. Further, when a toner image obtained by development is electrostatically transferred onto a transfer sheet, an insulating magnetic toner having high electrical resistance is generally used. [Problems to be solved by the invention] When reversal development is performed by charging the charged insulating magnetic toner as described above to the same polarity as the electrostatic latent image, the image quality is lower than that using a two-component developer. The reality is that it is inferior to what was done. In other words, when using magnetic toner that is charged to the same polarity as the electrostatic latent image, results equivalent to those using the two-component developer described above can be obtained in terms of image density, but in terms of resolution. There is a problem in that it is not sufficient and dust tends to occur around the image. The present invention solves the above-mentioned problems and aims to provide a reversal developing method that uses magnetic toner, has high resolution, and does not generate dust around the image. It is something. [Means for Solving the Problems] In order to solve the above problems, the following technical means were adopted in the present invention. That is, A. An electrostatic latent image is formed on the surface of an image carrier, and a non-magnetic conductive sleeve, which is disposed opposite to the surface of the image carrier and has a magnetic field generating member inside, is mainly composed of resin and magnetic powder. A magnetic toner is supplied, the magnetic toner is conveyed toward the image carrier surface by relative rotation between the sleeve and the magnetic field generating member, and a DC voltage is applied to the sleeve to form a non-image of the electrostatic latent image. In the reversal development method in which the magnetic toner is attached to the portion. B. Negative charging characteristics of the image carrier. C. The magnetic toner is capable of cold pressure fixing and has positive charging characteristics. D. Applying a negative DC voltage to the sleeve.
This is a technical measure taken. [Operation] FIG. 1 is a sectional view of essential parts showing an example of a developing device for carrying out the present invention. In the figure, reference numeral 1 denotes a photoreceptor drum, which consists of a photoconductive layer 1a holding an electrostatic latent image (indicated by the symbol - in the figure) and a conductive substrate 1b electrically grounded, and is directed in the direction of arrow W. Rotatably installed. Next, 2 is a toner tank which stores toner 3. A sleeve 4 is rotatably provided in the lower part of the toner tank 2 facing the photoreceptor drum 1, and a permanent magnet member 5 having a plurality of magnetic poles on its surface is coaxially arranged in the sleeve 4 and arranged in the direction indicated by the arrow X.
It is provided so that it can rotate independently in the direction. Reference numeral 6 denotes a doctor blade, which is provided so as to face the surface of the sleeve 4 so as to be able to come in and out at will, and is used to remove the toner 3 that moves on the sleeve 4.
Regulate the thickness of Next, the sleeve 4 is made of a non-magnetic and conductive material such as austenitic stainless steel or aluminum alloy, and is electrically connected to a DC power source 7 having negative polarity. A reversal development method using the above configuration will be described. First, by rotating the sleeve 4 and the permanent magnet member 5 relative to each other, the toner 3 contained in the toner tank 2 is pulled out onto the sleeve 4 and conveyed from the doctor gap d to the developing gap D in the direction of arrow Y. Toner 3 is in photoconductive bath 1
It has a property of being positively charged with a polarity opposite to that of the electrostatic latent image formed on a, and becomes positively charged by contact between the sleeve 4, the doctor blade 6, or the toner 3 during the conveyance process. When the positively charged toner 3 reaches the development area,
It adheres to the non-image areas of the photoconductive layer 1a to form a toner image. Next, this toner image reaches a transfer position by the rotation of the photoreceptor drum 1, and by applying a positive electric field with a polarity opposite to that of the electrostatic latent image from the back side of the transfer sheet (not shown), the toner image is transferred to the transfer position. transcribed on top;
Then, it is fixed by pressure fixing means. In the reversal development method of the present invention, since magnetic toner is used which is charged with a polarity opposite to that of the electrostatic latent image, the magnetic toner is thought to adhere to the image area of the electrostatic latent image. According to experiments conducted by the present inventors, it has been confirmed that the electrostatic latent image clearly adheres to the non-image area as described above, and the reproducibility is also sufficient. The reason why high quality images can be obtained by the present invention is as follows.
Although the details are unknown, it is assumed that the reason is as follows. In the process of conveying magnetic toner on the sleeve,
As described above, most toner particles are positively charged and have a positive charge. When this magnetic toner reaches the development area and enters the electric field of the electrostatic latent image,
Charges in the toner move according to the direction of the electric field, and toner particles near the interface with the photoreceptor, where the electrostatic latent image potential is low, become negatively charged. As a result, negatively charged toner particles adhere to non-image areas of the electrostatic latent image, resulting in a reversed image. Therefore, in the past, a magnetic toner charged to the same polarity as the electrostatic latent image was used, which caused an overdevelopment state. That is, too much toner adheres to the surface of the photoreceptor, resulting in dust. On the other hand, according to the present invention, only the toner near the interface with the photoreceptor has a charging polarity that contributes to development, so it is thought that overdevelopment can be suppressed and dust generation can be prevented. The magnetic toner used in the present invention has a triboelectric charge amount of 2 to 2 when measured by a blow-off method.
20μc/g, and the charging voltage on the sleeve is 5~
Preferably it is 60V. That is, when the amount of triboelectric charge and the charging voltage become excessive, the image density decreases, while when they are insufficient, fog increases, both of which are disadvantageous. Next, the magnetic powder constituting the magnetic toner includes alloys or compounds containing ferromagnetic elements such as iron, cobalt, and nickel, including ferrite and magnetite, and other materials that have been made ferromagnetic by heat treatment or some other treatment. Various alloys such as those shown may be used. These ferromagnetic materials are several μm to several tens of μm
Since it is contained in a toner having a particle size of 0.02 to 3 μm, it is desirable that the average particle size is 0.02 to 3 μm. Therefore, the amount contained in the toner is 30 to 70% of the total amount of toner.
It is desirable to set it as weight%. If it is less than 30% by weight, the magnetic force of the toner decreases and it becomes easy to scatter from the sleeve, while if it exceeds 70% by weight, the resin content becomes extremely low and the fixing properties are deteriorated, which is disadvantageous. Next, the magnetic toner used in the present invention can be fixed under cold pressure, and for example, the following resins are used. Namely, higher fatty acids, higher fatty acid metal salts, higher fatty acid derivatives, higher fatty acid amides, waxes, rosin derivatives, alkyd resins, epoxy-modified phenolic resins, natural resin-modified phenolic resins, amino resins, silicone resins, polyurethane, urea resins. , polyester resin, copolymerized oligomer of acrylic acid or methacrylic acid and long-chain alkyl acrylate, copolymerized oligomer of styrene and long-chain alkyl acrylate, long-chain alkyl methacrylate, polyolefin,
Examples include ethylene-vinyl acetate copolymers, ethylene-vinyl alkyl ether copolymers, maleic anhydride copolymers, petroleum residues, rubbers, and the like. Any of the above resins can be arbitrarily selected and mixed as desired, but those having a glass transition point exceeding 40° C. are effective in order not to reduce the fluidity when formed as a toner. In addition to the above, various pigments and/or additives used in general dry developers can be added. However, the content based on the total amount of the toner is suitably less than 10% by weight, taking into consideration the electrical properties of the toner. Pigments that can be used include, for example, carbon black, aniline blue, calco oil blue, chrome yellow, ultramarine blue, DuPont oil red, quinoline yellow, methylene blue chlorad, phthalocyanine blue, malachite green oxalate, lamp black, rose bengal and and mixtures thereof. Note that when the magnetic powder itself is colored, such as magnetite, there is no need to add it. In addition, when using carbon flux, in order not to reduce the insulation properties of the toner, it is necessary to
It is desirable to contain it in a range of 5 parts by weight. Next, the magnetic toner used in the present invention can be manufactured from the above-mentioned materials by a known method such as a pulverization method or a spray drying method. The average particle size of the toner to be produced is preferably in the range of 5 to 30 μm, preferably 10 to 20 μm. The electric resistance or fluidity can be adjusted by adding conductive particles such as carbon black or tin oxide or additives such as silica powder to the toner particle surface after classification. [Examples] The present invention will be specifically explained below using Examples, but the present invention is not limited to these Examples. Polyethylene wax (manufactured by Mitsui Petrochemical Industries)
HIWA×200P) and ethylene-vinyl acetate copolymer (ACP400 manufactured by Allied Chemical Co., Ltd.) mixed at a weight ratio of 7:3, magnetite (EPT500 manufactured by Toda Industries), and a positive charge control agent (Bontron No. manufactured by Orient Chemical Co., Ltd.). .1) were dry mixed according to the formulation shown in the table, and heated and kneaded in a kneader at a temperature of 200°C. The resulting kneaded product was cooled and solidified, and then ground into particles of 20 μm or less using a jet mill. Next, this pulverized powder was put into a super mixer, and 0.1 to 0.5 parts by weight of finely powdered silica (R972 manufactured by Nippon Aerosil Co., Ltd.) was added and mixed. The mixed powder was heat-treated by introducing it into a hot air stream at 120°C, and then classified using a zigzag classifier to obtain magnetic toner No. 1 with a particle size distribution of 5 to 20 μm. 1 to 4 were obtained. The triboelectric charge amount (hereinafter referred to as TEC) and surface potential of these magnetic toners are shown in the table. The TEC of the above-mentioned magnetic toner was measured using a commercially available blow-off powder charge measuring device (Toshiba Chemical TB-
200) under the following conditions. Carrier (Japan Iron Powder Z-200) 10g and toner 0.5g
was placed in a plastic container with an outer diameter of 40 mmφ, and rotated for 10 minutes using a flow surface angle measuring device. A 200 mg sample was taken from the resulting mixture and placed in a container using a 325 mesh sieve. The charge amount is measured using a charge measuring device under the conditions of a blow pressure of 1.0 Kg/mm 2 and a blow time of 40 seconds. In addition, the charging voltage of the toner, that is, the surface potential is the second
Measure with the equipment shown in the figure. In the same figure,
8 is a non-magnetic sleeve (outer diameter 50mmφ), 9 is a permanent magnet member (outer diameter 46mmφ, length 150mm, 12 poles symmetrical magnetization,
The magnetic flux density on the sleeve is 1000 G), 10 is a surface electrometer (Trek 344), and 11 is a probe. After adjusting the gap g between the sleeve 8 and the probe 11 to 5 mm, 3 g of toner was supplied onto the sleeve 8, and the surface potential of the toner was measured when the permanent magnet member 9 was rotated at 1000 rpm for 1 minute. do. Next, magnetic toner with different TEC and surface potential
No... Examples 5 to 7 were produced under the same conditions as in the above example. In addition, No. Magnetic toner No. 5 differs from other toners in that it uses a negative charge control agent (Bontron E81 manufactured by Orient Chemical Co., Ltd.).
本発明の反転現像方法は、以上記述のような構
成および作用であるから、高品質な画像が得ら
れ、特に解像度が高く、かつ画像周辺にチリが発
生することのない反転画像が得られるという効果
がある。
Since the reversal developing method of the present invention has the structure and operation described above, it is possible to obtain a high-quality image, and in particular, to obtain a reversal image that has high resolution and does not generate dust around the image. effective.
第1図は本発明を実施するための現像装置の一
例を示す断面図、第2図はトナーの表面電位測定
装置を示す断面図である。
1:感光体ドラム、3:トナー、4:スリー
ブ、5:永久磁石部材。
FIG. 1 is a sectional view showing an example of a developing device for carrying out the present invention, and FIG. 2 is a sectional view showing a toner surface potential measuring device. 1: Photosensitive drum, 3: Toner, 4: Sleeve, 5: Permanent magnet member.
Claims (1)
担体表面に対向して配置しかつ内部に磁界発生部
材を備えた非磁性導電性スリーブ上に樹脂と磁性
粉を主体とする磁性トナーを供給し、前記スリー
ブと前記磁界発生部材との相対的回転により前記
磁性トナーを前記画像担体表面に向かつて搬送
し、前記スリーブに直流電圧を印加して前記静電
潜像の非画像部に前記磁性トナーを付着させる反
転現像方法において、前記画像担体を負の帯電特
性とし、前記磁性トナーを冷間圧力定着可能であ
りかつ正帯電特性とし、かつ前記スリーブに負の
直流電圧を印加することを特徴とする反転現像方
法。 2 磁性トナーの摩擦帯電量が2〜20μc/g、
かつスリーブ上の帯電電圧が5〜60Vである特許
請求の範囲第1項記載の反転現像方法。[Scope of Claims] 1. An electrostatic latent image is formed on the surface of an image carrier, and resin and magnetic powder are placed on a non-magnetic conductive sleeve that is disposed opposite to the surface of the image carrier and has a magnetic field generating member inside. The magnetic toner is supplied as a main component, and the magnetic toner is conveyed toward the surface of the image carrier by relative rotation between the sleeve and the magnetic field generating member, and a DC voltage is applied to the sleeve to form the electrostatic latent image. In the reversal development method in which the magnetic toner is attached to a non-image area of the image carrier, the image carrier has a negative charging characteristic, the magnetic toner can be fixed under cold pressure and has a positive charging characteristic, and the sleeve is provided with a negative DC current. A reversal development method characterized by applying a voltage. 2 The amount of triboelectric charge of the magnetic toner is 2 to 20 μc/g,
The reversal developing method according to claim 1, wherein the charging voltage on the sleeve is 5 to 60V.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP604086A JPS62164055A (en) | 1986-01-14 | 1986-01-14 | Inverting developing method |
| DE19863640642 DE3640642A1 (en) | 1985-11-29 | 1986-11-28 | REVERSE DEVELOPMENT PROCEDURE |
| US07/185,242 US4865936A (en) | 1985-11-29 | 1988-04-18 | Electrophotographic reversal development method using magnetic field and specified development gap |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP604086A JPS62164055A (en) | 1986-01-14 | 1986-01-14 | Inverting developing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62164055A JPS62164055A (en) | 1987-07-20 |
| JPH0462667B2 true JPH0462667B2 (en) | 1992-10-07 |
Family
ID=11627523
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP604086A Granted JPS62164055A (en) | 1985-11-29 | 1986-01-14 | Inverting developing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62164055A (en) |
-
1986
- 1986-01-14 JP JP604086A patent/JPS62164055A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62164055A (en) | 1987-07-20 |
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